JP4422326B2 - Borderless via with a patterned metal layer gap-filled with HSQ - Google Patents
Borderless via with a patterned metal layer gap-filled with HSQ Download PDFInfo
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- JP4422326B2 JP4422326B2 JP2000516371A JP2000516371A JP4422326B2 JP 4422326 B2 JP4422326 B2 JP 4422326B2 JP 2000516371 A JP2000516371 A JP 2000516371A JP 2000516371 A JP2000516371 A JP 2000516371A JP 4422326 B2 JP4422326 B2 JP 4422326B2
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- layer
- hsq
- metal
- containing plasma
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- 229910052751 metal Inorganic materials 0.000 title claims description 94
- 239000002184 metal Substances 0.000 title claims description 94
- 229920003209 poly(hydridosilsesquioxane) Polymers 0.000 claims description 91
- 238000000034 method Methods 0.000 claims description 29
- 229920002120 photoresistant polymer Polymers 0.000 claims description 22
- 239000004065 semiconductor Substances 0.000 claims description 21
- 238000000151 deposition Methods 0.000 claims description 16
- 230000004888 barrier function Effects 0.000 claims description 15
- 239000004020 conductor Substances 0.000 claims description 12
- 229910008051 Si-OH Inorganic materials 0.000 claims description 11
- 229910006358 Si—OH Inorganic materials 0.000 claims description 11
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 claims description 11
- 239000000758 substrate Substances 0.000 claims description 10
- NMJKIRUDPFBRHW-UHFFFAOYSA-N titanium Chemical compound [Ti].[Ti] NMJKIRUDPFBRHW-UHFFFAOYSA-N 0.000 claims description 10
- 238000009832 plasma treatment Methods 0.000 claims description 9
- 239000002131 composite material Substances 0.000 claims description 7
- 238000005530 etching Methods 0.000 claims description 7
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 7
- 229910052721 tungsten Inorganic materials 0.000 claims description 7
- 239000010937 tungsten Substances 0.000 claims description 7
- 229910000838 Al alloy Inorganic materials 0.000 claims description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- 229910052782 aluminium Inorganic materials 0.000 claims description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 6
- 239000003870 refractory metal Substances 0.000 claims description 6
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 5
- 229910052719 titanium Inorganic materials 0.000 claims description 5
- 239000010936 titanium Substances 0.000 claims description 5
- 239000002318 adhesion promoter Substances 0.000 claims description 4
- MAKDTFFYCIMFQP-UHFFFAOYSA-N titanium tungsten Chemical compound [Ti].[W] MAKDTFFYCIMFQP-UHFFFAOYSA-N 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 239000006117 anti-reflective coating Substances 0.000 claims description 2
- 230000007423 decrease Effects 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 1
- 230000000149 penetrating effect Effects 0.000 claims 1
- 239000010410 layer Substances 0.000 description 83
- 238000005229 chemical vapour deposition Methods 0.000 description 9
- 230000015556 catabolic process Effects 0.000 description 7
- 238000006731 degradation reaction Methods 0.000 description 7
- 238000013461 design Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 230000008021 deposition Effects 0.000 description 5
- 238000010586 diagram Methods 0.000 description 5
- 238000012545 processing Methods 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000011810 insulating material Substances 0.000 description 3
- 238000001465 metallisation Methods 0.000 description 3
- 238000000059 patterning Methods 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 238000009834 vaporization Methods 0.000 description 3
- 230000008016 vaporization Effects 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 229910000881 Cu alloy Inorganic materials 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000000593 degrading effect Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000000206 photolithography Methods 0.000 description 2
- 238000005240 physical vapour deposition Methods 0.000 description 2
- 239000002574 poison Substances 0.000 description 2
- 231100000614 poison Toxicity 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000011800 void material Substances 0.000 description 2
- 229910001316 Ag alloy Inorganic materials 0.000 description 1
- 229910001020 Au alloy Inorganic materials 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 239000003353 gold alloy Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 229910021421 monocrystalline silicon Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 1
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- -1 structures Substances 0.000 description 1
- MNWRORMXBIWXCI-UHFFFAOYSA-N tetrakis(dimethylamido)titanium Chemical compound CN(C)[Ti](N(C)C)(N(C)C)N(C)C MNWRORMXBIWXCI-UHFFFAOYSA-N 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02109—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates
- H01L21/02112—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer
- H01L21/02123—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing silicon
- H01L21/02126—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing silicon the material containing Si, O, and at least one of H, N, C, F, or other non-metal elements, e.g. SiOC, SiOC:H or SiONC
- H01L21/02134—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing silicon the material containing Si, O, and at least one of H, N, C, F, or other non-metal elements, e.g. SiOC, SiOC:H or SiONC the material comprising hydrogen silsesquioxane, e.g. HSQ
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- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02225—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer
- H01L21/0226—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process
- H01L21/02263—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase
- H01L21/02271—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase deposition by decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition
- H01L21/02274—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase deposition by decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition in the presence of a plasma [PECVD]
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- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/027—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34
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- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/314—Inorganic layers
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- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76801—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing
- H01L21/76802—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing by forming openings in dielectrics
- H01L21/76816—Aspects relating to the layout of the pattern or to the size of vias or trenches
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- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76801—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing
- H01L21/76822—Modification of the material of dielectric layers, e.g. grading, after-treatment to improve the stability of the layers, to increase their density etc.
- H01L21/76826—Modification of the material of dielectric layers, e.g. grading, after-treatment to improve the stability of the layers, to increase their density etc. by contacting the layer with gases, liquids or plasmas
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- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76801—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing
- H01L21/76837—Filling up the space between adjacent conductive structures; Gap-filling properties of dielectrics
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- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/0001—Technical content checked by a classifier
- H01L2924/0002—Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00
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- Microelectronics & Electronic Packaging (AREA)
- General Physics & Mathematics (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Power Engineering (AREA)
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- Internal Circuitry In Semiconductor Integrated Circuit Devices (AREA)
- Formation Of Insulating Films (AREA)
Description
【0001】
【技術分野】
この発明は信頼性のある配線パターンを備える、高密度の多金属層半導体装置に関する。この発明は、特に、0.25ミクロン以下の設計部分を備える、高密度の多金属層半導体装置の製造に適用できる。
【0002】
【背景分野】
超大規模集積半導体装置に関する高密度化および高性能への要求の高まりによって、0.18ミクロンなどの0.25ミクロン以下の設計部分、より速いトランジスタおよび回路速度、高い信頼性および増大した製造処理量といったものが必要とされる。設計部分を0.25ミクロン以下に縮小することは、従来のフォトリソグラフィ、エッチングおよび堆積技術を含む従来の配線技術の限界に挑むことになる。
【0003】
パターニングされた金属層を形成するための従来の方法は、主な金属パターニング技術として、サブトラクティブ・エッチングまたはエッチバックステップを含む。そのような方法では、典型的には単結晶シリコンの半導体基板の上に第1の絶縁層が形成され、導電性コンタクトがソース/ドレイン領域などの半導体基板上の活性領域への電気的接続として、そこに形成される。アルミニウムまたはアルミニウム合金などの金属層が第1の絶縁層上に堆積され、所望の導電パターンに対応するパターンを有するフォトレジストマスクが金属層上に形成される。金属層はフォトレジストマスクを介してエッチングされ、間に配線スペースを備える複数の金属線などのような、間隙によって隔てられる金属部分を含む導電性パターンが形成される。次に、絶縁層が結果としてできた導電性パターンに加えられ、間隙を充填し、表面が平坦化される。この際、従来のエッチングまたは化学的機械研磨(CMP)平坦化技術などが用いられる。
【0004】
図1および2に示されるように、従来技術は、典型的にはトランジスタ(図示せず)を備える活性領域を含む半導体基板上に形成される絶縁層10上への金属層11の堆積を含む。フォトリソグラフィ後、その間に間隙を備える金属部分11a、11b、11cおよび11dを含むパターニングされた金属層を形成する。典型的には、スピン・オン・ガラス(SOG)などの絶縁材料12が金属部分間の間隙を充填するように堆積され、約300℃から約350℃の温度でベークされ、利用される特定のSOG材料によるが、最高約1時間の間、約350℃から約400℃で垂直炉の中で硬化されて、平坦化を果たす。プラズマCVD(PECVD)によって別の酸化物が堆積され、CMPなどによって平坦化が行なわれる。
【0005】
たとえば金属線および配線スペースの部分の大きさを0.2ミクロン以下に縮小すると、ボイドなしに配線間隔を満足に充填し、適当なステップカバレッジを得ることはますます困難になる。信頼性のある配線構造を形成することもまたますます困難になる。間隙充填のためのスピンオン絶縁材料が唯一の実行可能な解決策のようである。絶縁層にスルーホールが形成され、下部にある金属部分を露出すると、金属部分はスルーホールの底部全体を占める取付け台としての役割を果たす。金属プラグなどの導電性金属でスルーホールを充填して導電性バイアを形成すると、導電性バイアの底部表面全体が金属部分と直接接触する。そのような従来技術は図3に示される。ここでは第1のパターニングされた金属層の金属部分30が第1の絶縁層31上に形成され、第2の絶縁層33中に形成されるスルーホール32によって露出される。従来技術例によると、金属部分30がその底部開口部全体を囲むようスルーホール32が形成され、これによってスルーホール32を充填して導電性バイア35を形成する金属プラグ34にとっての、取付け台としての役割を果たす。このようにして導電性バイア35の底部表面全体が金属部分30と直接接触する。導電性バイア35は、金属部分30と第2のパターニングされた金属層の一部である金属部分36とを電気的に接続する。図2および3に示されるように、金属部分または導線の側面端、たとえば30A、30Bと36Aおよび36Bとは、エッチングの結果幾分先細りになる。
【0006】
設計部分を0.25ミクロン以下の範囲に縮小することは、著しい高密度化を要求する。導電性バイアの底部表面を完全に囲む取付け台を形成するという従来技術では、半導体チップ上のかなりの貴重なスペースが使用され、これは高まる高密度化要求に反する。さらに、そのような削減された大きさを有するスルーホールをボイドなしに充填することは、極めて困難である。なぜならアスペクト比、すなわちスルーホール直径に対するスルーホールの高さ、が極めて高いからである。したがって従来の改良技術は、アスペクト比を減少させるように、意図的なスルーホールの直径の拡大を含む。その結果、導電性バイアの底部表面が下にある金属部分によって完全に囲まれないという、不整列が起こる。この型のバイアは「ボーダレスバイア」と呼ばれ、チップのスペースを節約する。
【0007】
しかしながら、ボーダレスバイアの使用は新しい問題を生み出す。たとえば、SOGの不安定性および低密度によって、不整列のスルーホールが形成されるとき、不整列の結果として、SOG間隙充填層がエッチングによって貫通される。そのような貫通の結果、水分とガスが蓄積することによって配線の抵抗が増大する。その上、スパイクが起こり得る。すなわち金属プラグの基板への貫通が短絡をもたらす。図4に言及する。第1の絶縁層41が基板40上に形成され、反射防止膜45Aを含むたとえば金属線45などの第1の金属部分を含む第1の金属パターンが、第1の絶縁層41上に形成され、間隙はSOG42で充填される。次に、絶縁層43が堆積され、そこに形成される不整列のスルーホールが、金属線45の上部表面の一部および側部表面の少なくとも一部を露出し、SOG層42の一部を貫通して露出する。スルーホールを、典型的には最初は障壁層(図示せず)およびタングステンを含む金属プラグ44で充填すると、スパイクが起こる。すなわち基板40への貫通によって短絡が起きる。
【0008】
この発明では、SOGをハイドロゲンシラセスキオキサン(HSQ)に取り替え、これは配線パターンの使用に多くの利点を供する。HSQは比較的炭素がないことによりポイズンドバイアの問題を回避する。その上、炭素が実質上存在しないため、短絡を回避するように、HSQを金属線の上部表面より下にエッチバックする必要がない。さらにHSQは、優れた平坦性を示し、従来のスピン・オン装置を利用して0.15ミクロン未満の配線スペースの間隙を充填することができる。HSQはおよそ200℃で溶解相に入るが、高い絶縁性の一定したガラス相に転換するのは、金属間の用途では約400℃の温度で、プリメタルの用途では約700℃ないし約800℃に達してからである。1998年8月31日出願の同時係属中の出願連続番号PCT/US98/18012号において、金属部分に隣接する堆積されたHSQ層の部分を選択的に加熱し、ボーダレスバイア用の不整列のスルーホールをエッチングするときに、隣接する部分を貫通しにくくさせる方法が、開示されている。
【0009】
しかしながら、HSQは加工中に劣化を受けやすく、ボーダレスバイアの形成時のボイドなどのさまざまな問題に至る。たとえば、ボーダレスバイアを形成するとき、フォトレジストマスクが堆積され、不整列のスルーホールがエッチングされると、金属線の上部表面の一部および側部表面の一部を露出し、HSQ層を貫通して露出する。次に、典型的には酸素(O2)含有プラズマを利用して、フォトレジストマスクが除去される。ボーダレスバイアを含む配線パターンにおける間隙充填のためのHSQ利用の実行可能性を評価する実験中、フォトレジストマスクを除去するために利用されたO2含有プラズマが、HSQ層を劣化させることが判明した。窒化チタンまたはチタン−窒化チタンなどの障壁材料などで不整列のスルーホールをその後充填すると、スパイクが起こった。すなわち、障壁材料がHSQ層を抜けて基板または下にある導電性部分まで貫通した。
【0010】
HSQは、典型的には、約70%ないし約90%のSi−H結合を含有する。しかしながら、O2含有プラズマへさらすと、かなりの数のSi−H結合が破壊され、Si−OH結合が形成される。O2含有プラズマで処理すると、堆積されたHSQ膜内に約20%ないし約30%ものSi−H結合が残った。さらに、O2含有プラズマにさらすと、堆積された直後のHSQ膜の水分含有量およびその水分を吸収する傾向が増大した。Si−H結合が減少しSi−OH結合が高いHSQ膜は、周囲から水分を吸収する傾向があり、水分が後の障壁金属堆積中気化放出される。このようにして、その後のたとえば、チタン−窒化チタンおよびタングステンなどの障壁および金属堆積中、気化放出が起こり、それによってボイドを生じ不完全な電気的接続に至ることが判明した。
【0011】
HSQの明白な利点を鑑みると、ボーダレスバイアを含む配線パターンの形成において、ボイドのない間隙充填のためにHSQが利用され得る技術を提供する必要がある。
【0012】
【発明の開示】
この発明の目的は、0.25ミクロン以下の設計部分および完成度の高いボーダレスバイアを含む配線パターンを備える高密度多金属層半導体装置の製造方法である。
【0013】
この発明の他の目的は、完成度の高いボーダレスバイアを含む配線パターンを含む、0.25ミクロン以下の設計部分を備える高密度多金属層半導体装置である。
【0014】
この発明のさらなる目的、利点および他の特徴は、以下の明細書において部分的に説明され、かつ以下の検討により当業者には部分的に明らかになるか、または、この発明の実施から習得される。添付の特許請求の範囲において特に指摘されるように、この発明の目的と利点とは実現され獲得され得る。
【0015】
この発明によれば、前記および他の目的は以下のものを含む半導体装置の製造方法によって部分的に達成される。すなわち、Si−H結合を含有するハイドロゲンシラセスキオキサン(HSQ)を含む絶縁層を堆積するステップと、H2含有プラズマで堆積されたHSQ層を処理し、Si−H結合数を増加させるステップとを含む。
【0016】
この発明の他の局面は、以下のものを有する配線パターンを含む半導体装置である。すなわち、第1の下部金属部分と第2の上部金属部分との間に電気的接続を形成する導電性材料で充填された開口部と、第1の金属部分および導電性材料に隣接するハイドロゲンシラセスキオキサン(HSQ)の層とを含み、HSQの層は約70%を超えるSi−H結合を含む。
【0017】
この発明のさらなる目的と利点とは、この発明を実施するために意図された最良の形態を単に例示することによりこの発明の好ましい実施例のみが示され記載される以下の詳細な説明から、当業者には、容易に明らかとなるであろう。この発明は他の異なる実施が可能であり、そのいくつかの詳細は、この発明から全く逸脱することなく、さまざまな明らかな点において修正が可能であることが理解される。したがって、図面と明細書は全く例示的であり、限定的でないものとみなされる。
【0018】
【発明を実施する最良の形態】
この発明によって、HSQ層の劣化より派生する悪影響を被ることなく、パターニングされた金属層の間隙を充填するHSQを利用して、0.25ミクロン以下の設計部分を有する高密度の多金属層半導体装置の形成において、信頼性の高いボーダレスバイアの有効な使用が可能となる。たとえば、チタン−窒化チタンまたは窒化チタンなど、最初に障壁材料を含む複合プラグでスルーホールを充填する前に、レジスト除去中、O2含有プラズマに晒すと、堆積されたHSQは劣化される。
【0019】
HSQは、従来のスピン・オン装置を利用して、優れた平坦性と間隙充填能力を示すという点で、非常に所望される間隙充填のための絶縁材料である。HSQは容易に、たとえば約0.15ミクロ未満の配線スペースの間隙を充填し得る。その上、無炭素高分子前駆物質の使用により、ポイズンドバイアの問題に直面せず、HSQは金属線の上部表面より下にエッチバックされる必要がない。HSQの一つの形状が、フロワブル・オキサイド(Flowable OxideTMまたはFox TM)の製品名でダウ・コーニング社(Dow Corning Corp.)により商業的入手が可能である。
【0020】
HSQは、主に、たとえば約70%ないし約90%のSi−H結合を含有する。しかしながら、HSQは処理中に劣化されやすく、それによって、Si−H結合の数が大きく減少する。たとえばフォトレジスト除去中、O2含有プラズマに晒すと、約20%から約30%だけ、HSQのSi−H結合の数が減少し、Si−OH結合数が増加する。その結果、そのような劣化したHSQは周囲から水分を吸収するという性質を示す。従来のHI−VACスパッタ・チャンバ内でチタン−窒化チタン障壁層をスパッタ堆積するときのように、その後にスルーホールを充填してボーダレスバイアを形成する間、そのような吸収された水分は気化放出され、それによってボイドが生じ、装置の信頼性を低下させる。たとえば、1997年12月18日出願の係属中の米国特許出願連続番号第08/992,430号に開示される方法などによる化学的気相蒸着によって、窒化チタンを堆積するときにも、気化放出は起こる。
【0021】
この発明によると、O2含有プラズマへの露出により起こる堆積された直後のHSQの劣化は、実質的に逆転される、すなわち、劣化したHSQはH2含有プラズマで処理することにより、その堆積された直後の状態へ実質的に回復される。たとえば、劣化したHSQをH2/N2含有プラズマなどのH2含有プラズマで処理すると、Si−H結合の数は、約70%を超え、たとえば約87%ないし約90%、約80%を超えて、実質的に増加することが判明した。劣化したHSQをH2/N2含有プラズマ中で処理すると、結果として、O2含有プラズマへの露出中に破壊または減少したSi−H結合が実質的に回復することも判明した。劣化したHSQをH2/N2プラズマで処理すると、O2含有プラズマへの露出によって生じるSi−OH結合が、実質的に減少することも、さらに判明した。堆積された直後の状態へ実質的に回復すると、この発明によるH2含有プラズマで処理されたHSQは、周囲から水分を吸収するという重大な性質を示さない。
【0022】
このようにして、この発明によると、劣化したHSQで間隙充填された層は、実質的に元のSi−H結合含有量に回復され、周囲から多くの水分を吸収するという性質はもはやない。したがって、その後の導電性材料でのスルーホールの充填の際に気化放出およびボイドが起こらない。
【0023】
従来は、H2/N2プラズマ処理を利用して、化学気相蒸着法(CVD)によって堆積された窒化チタン膜を処理し、炭素含有量を減少させてきた。たとえば、1997年12月18日出願の、同時係属中の米国特許出願連続番号第08/992,430号を参照。また、エイ・ジェイ・コノクニ(A. J. Konecni)らによる「障壁/接着層適用のための、安定したプラズマ処理されたCVD窒化チタン膜」第181−183頁、1996年6月18日−20日、VMIC大会、1996ISMICと、キム(Kim)らによる「テトラキス−ジメチルアミノチタンを用いる化学気相蒸着法によるTiN膜の安定性」、電気化学学会誌、第143巻第9号、1996年9月、第L188頁−L190頁と、ジェイ・ラコポニ(J. Lacoponi)らによる「その場的窒素プラズマによるCVDTiNの抵抗性向上および低抵抗多層配線におけるその応用」、1995年、ULSI応用のための先進メタライゼーションおよび配線システム、とを参照。
【0024】
この発明によるH2含有プラズマ処理を行なう際、当業者は関連するパラメータを最適化し、堆積されたHSQ膜のSi−H結合の数を増加させ、生じたSi−OH結合の数を減少させるという、開示された目的を達成することができる。たとえば、CVD窒化チタン膜の処理において、その炭素含有量と抵抗とを減少させるのに利用されるパラメータおよび条件は、劣化したHSQを処理してSi−H結合の数を増加させ、発生したSi−OH結合の数を減少させるのに有効である。したがって、1997年12月18日出願の米国特許出願連続番号第08/992,430号に開示されるパラメータ、同様に、前記コノクニら、キムら、ラコポニらによる刊行物に開示されるパラメータがこの発明に利用され得る。この発明によって劣化したHSQ層をH2/N2プラズマで処理する際、HSQの膜の厚さによるが、約300sccmの水素フロー、約200sccmの窒素フロー、約450℃の温度、約1.3Torrの気圧、約750WのRF出力および約25から約45秒の時間を利用することが好適であることが判明している。
【0025】
この発明の実施例によるボーダレスバイアの形成方法は、半導体基板上の第1の絶縁層を形成するステップと、第1の絶縁層上の第1の金属層をパターニングして配線スペースによって隔てられる金属線などの、間隙によって隔てられる金属部分を形成するステップとを含む。次にSOGに利用される従来のスピン装置を用いてスピンなどして、たとえば約200℃の適当な温度で、HSQを堆積することにより、間隙が充填される。HSQは、0.15ミクロン未満の間隙さえも、完全にボイドなしに容易に充填することができる。次に、第2の絶縁層が第1のパターニングされた金属層およびHSQ層上に堆積される。次に、不整列のスルーホールが第2の絶縁層中に形成され、部分的にHSQ層を貫通して、第1の金属層の側面表面の少なくとも一部および上部表面の一部とHSQ層の一部とを露出する。
【0026】
第2の絶縁層上にフォトレジストマスクを堆積し、フォトレジストマスクおよびHSQ層の一部を介してエッチングすることによって、スルーホールは、形成される。フォトレジストマスクは、従来の方法で、O2含有プラズマを利用して除去され、これによりHSQ層は劣化する。劣化したHSQ層は、劣化していない堆積された直後のHSQ層に比べて、著しく少ないSi−H結合と著しく多いSi−OH結合とを含む。さらに、O2含有プラズマに晒されると、劣化したHSQ膜は水分の含有量の増加を示し、周囲から水分を吸収することにより水分含有量は増加し続ける。
【0027】
O2含有プラズマでフォトレジストマスクを除去した後、劣化したHSQ層はH2/N2含有プラズマで処理され、これによりSi−H結合の数は著しく増加し、Si−OH結合の数は著しく減少する。さらに、H2含有プラズマでの処理中、HSQの水分含有量は減少し、処理されたHSQは水分を吸収するという重大な性質を示さない。O2含有プラズマへ晒すことによってもたらされる劣化を逆転することによって、HSQ層を実質的に回復して次に、不整列のスルーホールは、たとえば複合プラグなどの導電性材料で充填される。最初に、チタン、窒化チタン、チタン−タングステンまたはチタン−窒化チタンの障壁が堆積され、これが、主なプラグ材料の構成要素となる、その後に堆積されるタングステンにとっての付着促進物の役割を果たす。従来のスパッタリング装置を利用して、たとえば、チタン−窒化チタンの障壁材料はスパッタ堆積される。
【0028】
この発明の別の実施例では、1997年12月18日出願の米国特許出願連続番号第08/992,430号に開示される方法に従って、CVD−TiN障壁層が堆積される。この実施例の利点は、HSQ膜のH2/N2プラズマ処理および堆積されたCVD−TiN膜のH2/N2プラズマ処理が同じチャンバ内で行なわれ得ることである。
【0029】
この発明の実施例の概略図が図5に示される。パターニングされた金属層の金属部分51は、絶縁層50上に堆積され、その上に反射防止膜51を備える。金属部分間の間隙は、HSQ52で充填される。次に、酸化物53、典型的にはTEOS(テトラエチルオルソシリケート)から得られる酸化物が堆積され、CMPが行なわれる。次に、第2の絶縁層54が堆積され、その上にフォトレジストマスクが形成される。次に、エッチングが行なわれ、不整列のスルーホール55を形成し、これはHSQ層52を貫通し金属部分51の側面表面の一部を露出させる。スルーホール55の形成後、利用されたフォトレジストマスクが、O2含有プラズマを用いるような従来の方法で除去され、それにより、HSQ層52が劣化する。劣化は、典型的には、多くのSi−H結合の減少、かなりの数のSi−OH結合の形成および水分を吸収するという不所望の傾向を特徴とし、これによって、導電性材料でスルーホールを充填する際、気化放出によってボイドが発生する。
【0030】
この発明では、劣化したHSQ層はH2含有プラズマに晒され、それによって、Si−H結合の数を著しく増加させ、Si−OH結合の数を著しく減少させることにより、劣化したHSQ層を回復させる。さらに、回復されたHSQは周囲からあまり水分を吸収しなくなる。次に、タングステン56にとっての付着促進物としての役割を果たす障壁層57を最初に堆積するなどして、スルーホール55は複合プラグで充填される。障壁層は、典型的には、チタン、窒化チタン、チタン−タングステンまたはチタン−窒化チタンなどの高融点金属である。
【0031】
導電性バイア57を形成した後、第2のパターニングされた金属層が第2の絶縁層54上に形成される。この第2の金属層は、その上に反射防止膜58Aを備える金属部分58を含み、導電性バイア57を介して金属部分51に電気的に接続される。たとえば、5層の金属層などの、所望の数のパターニングされた金属層が形成され、間隙が充填されるまで、HSQを利用して第2のパターニングされた金属層を間隙充填し、H2含有プラズマ処理を行なうことにより、この方法が繰返される。
【0032】
この発明に利用される金属層は、従来例と一致し、典型的にはアルミニウムまたはアルミニウム合金を含む。この発明の実施例は、最初にはタングステン、チタンまたは窒化チタンなどの高融点金属層と、中間のアルミニウムまたはアルミニウム合金層と、チタン−窒化チタンなどの上部反射防止膜とを含む、複合のパターニングされた金属層の形成を含む。この発明では、従来のCVD技術によって、タングステンが堆積される。
【0033】
この発明は、半導体装置のさまざまな型、特に微細部分、特に、0.25ミクロン以下の微細部分を備える高密度多金属のパターニングされた層に適用でき、高速特徴および向上した信頼性を示す。この発明は、HSQの有利な利用を可能にし、O2含有プラズマへの露出などによって起こる、処理によって誘発される劣化という悪影響なしに、パターニングされた金属層を間隙充填することができる。このようにして、この発明は、ボーダレスバイア形成中のHSQにおけるボイド形成の問題を解決する。この発明は費用効率が高く従来の加工および装置に容易に統合され得る。
【0034】
この発明の実施例の実施においては、金属層は、アルミニウム、アルミニウム合金、銅、銅合金、金、金合金、銀、銀合金、高融点金属、高融点金属合金および高融点金属化合物などの半導体装置製造に典型的に利用されるいかなる金属からも、形成され得る。この発明の金属層は、半導体装置の製造に従来利用されるいかなる技術によっても形成され得る。たとえば、金属層は、従来の物理気相蒸着法(PVD)または化学気相蒸着法(CVD)およびたとえば銅および銅合金の電気めっきなどの従来のメタライゼーション技術によって形成され得る。
【0035】
以上の説明では、この発明の完全な理解を提供するために、具体的な材料、構造、化学製品、方法などの多くの具体的な詳細が述べられる。しかしながら、当業者なら理解するであろう通り、この発明は、具体的に述べられる詳細に頼ることなく、実施され得る。他の場合には、この発明を不必要に不明瞭にしないために周知の加工構成は記載されない。
【0036】
この発明の好ましい実施例のみおよびその多様性の一例がこの開示に示され述べられる。この発明は、さまざまな他の組合せと環境において使用が可能であり、ここに表わされるような発明の概念の範囲内で変更や変形が可能であることが、理解されるべきである。
【図面の簡単な説明】
【図1】 従来のパターニングされた金属層の間隙充填を例示する概略図である。
【図2】 従来のパターニングされた金属層の間隙充填を例示する概略図である。
【図3】 従来の金属プラグバイア配線を例示する概略図である。
【図4】 ボーダレスバイアにおけるスパイクを例示する概略図である。
【図5】 この発明によって形成されるボーダレスバイアを例示する概略図である。[0001]
【Technical field】
The present invention relates to a high-density multi-metal layer semiconductor device having a reliable wiring pattern. The present invention is particularly applicable to the manufacture of a high-density multi-metal layer semiconductor device having a design portion of 0.25 microns or less.
[0002]
[Background]
Higher density and higher performance requirements for ultra-large scale integrated semiconductor devices have resulted in sub-0.25 micron design features such as 0.18 micron, faster transistors and circuit speeds, higher reliability and increased manufacturing throughput. Is required. Reducing the design portion to 0.25 microns or less challenges the limitations of conventional wiring technologies, including conventional photolithography, etching and deposition techniques.
[0003]
Conventional methods for forming a patterned metal layer include a subtractive etch or etchback step as the main metal patterning technique. In such a method, a first insulating layer is typically formed on a single crystal silicon semiconductor substrate, and the conductive contacts serve as electrical connections to active regions on the semiconductor substrate, such as source / drain regions. Formed there. A metal layer such as aluminum or aluminum alloy is deposited on the first insulating layer, and a photoresist mask having a pattern corresponding to the desired conductive pattern is formed on the metal layer. The metal layer is etched through a photoresist mask to form a conductive pattern including metal portions separated by a gap, such as a plurality of metal lines with wiring spaces in between. Next, an insulating layer is added to the resulting conductive pattern, filling the gaps and planarizing the surface. At this time, a conventional etching or chemical mechanical polishing (CMP) planarization technique is used.
[0004]
As shown in FIGS. 1 and 2, the prior art typically includes the deposition of a metal layer 11 on an
[0005]
For example, if the size of the metal wire and the wiring space is reduced to 0.2 microns or less, it becomes more difficult to satisfactorily fill the wiring interval without voids and obtain appropriate step coverage. It is also increasingly difficult to form a reliable wiring structure. A spin-on insulating material for gap filling appears to be the only viable solution. When a through hole is formed in the insulating layer and a lower metal portion is exposed, the metal portion serves as a mounting base that occupies the entire bottom of the through hole. When a conductive via is formed by filling a through hole with a conductive metal such as a metal plug, the entire bottom surface of the conductive via is in direct contact with the metal portion. Such prior art is shown in FIG. Here, the
[0006]
Reducing the design portion to a range of 0.25 microns or less requires a significant increase in density. The prior art of forming a mount that completely encloses the bottom surface of the conductive vias uses a significant amount of valuable space on the semiconductor chip, which is contrary to increasing density requirements. Furthermore, it is extremely difficult to fill through holes having such a reduced size without voids. This is because the aspect ratio, that is, the height of the through hole with respect to the through hole diameter is extremely high. Thus, conventional improved techniques include intentional through-hole diameter enlargement to reduce the aspect ratio. As a result, misalignment occurs where the bottom surface of the conductive via is not completely surrounded by the underlying metal portion. This type of via is called a “borderless via” and saves chip space.
[0007]
However, the use of borderless vias creates new problems. For example, when misaligned through holes are formed due to SOG instability and low density, the SOG gap fill layer is etched through as a result of misalignment. As a result of such penetration, the resistance of the wiring increases due to the accumulation of moisture and gas. In addition, spikes can occur. That is, the penetration of the metal plug into the substrate causes a short circuit. Reference is made to FIG. A first
[0008]
In the present invention, SOG is replaced with hydrogen silsesquioxane (HSQ), which provides many advantages for the use of wiring patterns. HSQ avoids the poison via problem by being relatively carbon-free. Moreover, since there is virtually no carbon, it is not necessary to etch back the HSQ below the top surface of the metal line to avoid short circuits. Furthermore, HSQ exhibits excellent flatness and can fill gaps in the wiring space of less than 0.15 microns using conventional spin-on devices. HSQ enters the melt phase at approximately 200 ° C., but converts to a highly insulating constant glass phase at temperatures of about 400 ° C. for intermetallic applications and about 700 ° C. to about 800 ° C. for premetal applications. It is after reaching. In co-pending application serial number PCT / US98 / 18012 filed Aug. 31, 1998, selectively heats a portion of the deposited HSQ layer adjacent to a metal portion to provide an unaligned slew for a borderless via. A method for making it difficult to penetrate adjacent portions when etching holes is disclosed.
[0009]
However, HSQ is susceptible to degradation during processing, leading to various problems such as voids during the formation of borderless vias. For example, when forming a borderless via, when a photoresist mask is deposited and misaligned through holes are etched, a portion of the top and side surfaces of the metal lines are exposed and penetrate the HSQ layer And exposed. Next, the photoresist mask is removed, typically using an oxygen (O 2 ) containing plasma. During an experiment evaluating the feasibility of using HSQ for gap filling in wiring patterns including borderless vias, it was found that the O 2 containing plasma used to remove the photoresist mask degrades the HSQ layer. . Spikes occurred when subsequently filling misaligned through holes, such as with a barrier material such as titanium nitride or titanium-titanium nitride. That is, the barrier material penetrated through the HSQ layer to the substrate or underlying conductive portion.
[0010]
HSQ typically contains about 70% to about 90% Si-H bonds. However, exposure to an O 2 containing plasma destroys a significant number of Si—H bonds and forms Si—OH bonds. Treatment with an O 2 containing plasma left about 20% to about 30% Si—H bonds in the deposited HSQ film. Furthermore, exposure to O 2 containing plasma increased the moisture content of the HSQ film immediately after deposition and its tendency to absorb the moisture. HSQ films with reduced Si-H bonds and high Si-OH bonds tend to absorb moisture from the surroundings, and moisture is vaporized and released during subsequent barrier metal deposition. In this way, it was found that during subsequent barrier deposition and metal deposition such as, for example, titanium-titanium nitride and tungsten, vaporization emission occurred, thereby creating voids and leading to incomplete electrical connections.
[0011]
In view of the obvious advantages of HSQ, there is a need to provide a technique in which HSQ can be utilized for void-free gap filling in the formation of wiring patterns including borderless vias.
[0012]
DISCLOSURE OF THE INVENTION
An object of the present invention is a method for manufacturing a high-density multi-metal layer semiconductor device having a wiring pattern including a design portion of 0.25 microns or less and a borderless via having a high degree of perfection.
[0013]
Another object of the present invention is a high-density multi-metal layer semiconductor device having a design portion of 0.25 microns or less, including a wiring pattern including a borderless via having a high degree of completion.
[0014]
Additional objects, advantages and other features of the invention will be set forth in part in the description which follows, and in part will become apparent to those skilled in the art from the following discussion or may be learned from practice of the invention. The The objects and advantages of the invention may be realized and obtained as particularly pointed out in the appended claims.
[0015]
According to the present invention, the above and other objects are partially achieved by a method of manufacturing a semiconductor device including the following. A step of depositing an insulating layer containing hydrogen silsesquioxane (HSQ) containing Si—H bonds; a step of treating the HSQ layer deposited with H 2 containing plasma to increase the number of Si—H bonds; including.
[0016]
Another aspect of the present invention is a semiconductor device including a wiring pattern having the following. That is, an opening filled with a conductive material that forms an electrical connection between a first lower metal portion and a second upper metal portion, and a hydrogen silice adjacent to the first metal portion and the conductive material. A layer of skioxane (HSQ), the layer of HSQ containing more than about 70% Si-H bonds.
[0017]
Further objects and advantages of this invention will become apparent from the following detailed description, in which only preferred embodiments of the invention are shown and described, merely by way of illustration of the best mode contemplated for carrying out the invention. It will be readily apparent to the merchant. It will be understood that the invention is capable of other different implementations, and its several details are capable of modifications in various obvious respects, all without departing from the invention. Accordingly, the drawings and specification are to be regarded as illustrative in nature and not as restrictive.
[0018]
BEST MODE FOR CARRYING OUT THE INVENTION
The present invention provides a high density multi-metal layer semiconductor having a design portion of 0.25 microns or less utilizing HSQ that fills the gaps in the patterned metal layer without incurring the adverse effects derived from degradation of the HSQ layer. A highly reliable borderless via can be used effectively in forming the device. For example, exposure to an O 2 containing plasma during resist removal prior to filling the through hole with a composite plug that initially includes a barrier material, such as titanium-titanium nitride or titanium nitride, degrades the deposited HSQ.
[0019]
HSQ is a highly desired insulating material for gap filling in that it uses a conventional spin-on device and exhibits excellent flatness and gap filling capability. HSQ can easily fill gaps in wiring space, for example, less than about 0.15 micron. Moreover, due to the use of carbon-free polymer precursors, the poison via problem is not encountered and the HSQ does not need to be etched back below the upper surface of the metal line. One form of HSQ are possible commercially available by flowable Oxide Dow Corning under the product name (Flowable Oxide TM or Fo x TM) (Dow Corning Corp. ).
[0020]
HSQ mainly contains, for example, about 70% to about 90% Si—H bonds. However, HSQ is prone to degradation during processing, thereby greatly reducing the number of Si-H bonds. For example, exposure to an O 2 -containing plasma during photoresist removal reduces the number of Si—H bonds in HSQ by about 20% to about 30% and increases the number of Si—OH bonds. As a result, such degraded HSQ exhibits the property of absorbing moisture from the surroundings. Such absorbed moisture is vaporized and released during subsequent filling of the through-holes to form borderless vias, such as when sputter depositing a titanium-titanium nitride barrier layer in a conventional HI-VAC sputter chamber. Thereby creating voids that reduce the reliability of the device. For example, vapor deposition may also occur when depositing titanium nitride by chemical vapor deposition, such as by the method disclosed in pending US patent application Ser. No. 08 / 992,430, filed Dec. 18, 1997. Will happen.
[0021]
According to the present invention, the degradation of HSQ immediately after deposition caused by exposure to an O 2 containing plasma is substantially reversed, ie, the degraded HSQ is deposited by treatment with an H 2 containing plasma. It is substantially recovered to the state immediately after. For example, when degraded HSQ is treated with an H 2 containing plasma, such as an H 2 / N 2 containing plasma, the number of Si—H bonds exceeds about 70%, for example about 87% to about 90%, about 80%. Beyond that, it was found to increase substantially. It has also been found that treatment of degraded HSQ in a H 2 / N 2 containing plasma results in substantial recovery of broken or reduced Si—H bonds during exposure to the O 2 containing plasma. If the degraded HSQ is treated with H 2 / N 2 plasma, Si-OH bonds caused by exposure to O 2 containing plasma, also be substantially reduced, further proved. Upon substantial recovery to the state immediately after deposition, the HSQ treated with the H 2 containing plasma according to the present invention does not exhibit the critical property of absorbing moisture from the surroundings.
[0022]
Thus, according to the invention, the gap-filled layer with degraded HSQ is substantially restored to its original Si-H bond content and no longer has the property of absorbing much moisture from the surroundings. Therefore, vaporization emission and void do not occur during subsequent filling of the through hole with the conductive material.
[0023]
Conventionally, a titanium nitride film deposited by chemical vapor deposition (CVD) has been treated using H 2 / N 2 plasma treatment to reduce the carbon content. See, for example, co-pending US Patent Application Serial No. 08 / 992,430, filed December 18, 1997. Also, AJ Konecni et al., “Stable Plasma Treated CVD Titanium Nitride Films for Barrier / Adhesive Layer Application,” pages 181-183, June 18-20, 1996. VMIC Convention, 1996 ISMIC, and Kim et al., “Stability of TiN Films by Chemical Vapor Deposition Using Tetrakis-Dimethylamino Titanium”, Journal of Electrochemical Society, Vol. 143, No. 9, September 1996, Pp. L188-L190 and J. Lacoponi et al., “In-situ nitrogen plasma enhanced resistance of CVDTiN and its application in low resistance multilayer interconnects”, 1995, Advanced Meta for ULSI applications. See also Rization and Wiring System.
[0024]
When performing containing H 2 plasma treatment according to the present invention, as those skilled in the art to optimize the related parameters, increasing the number of Si-H bonds of the deposited HSQ film, reducing the number of the resulting Si-OH bonds The disclosed object can be achieved. For example, in the processing of CVD titanium nitride films, the parameters and conditions utilized to reduce the carbon content and resistance are such that the degraded HSQ is processed to increase the number of Si-H bonds and the generated Si Effective for reducing the number of —OH bonds. Therefore, the parameters disclosed in U.S. Patent Application Serial No. 08 / 992,430 filed December 18, 1997, as well as those disclosed in the publications by Konokuni et al., Kim et al., Lakoponi et al. Can be used in the invention. When the HSQ layer deteriorated according to the present invention is treated with H 2 / N 2 plasma, depending on the thickness of the HSQ film, the hydrogen flow is about 300 sccm, the nitrogen flow is about 200 sccm, the temperature is about 450 ° C., and the temperature is about 1.3 Torr. It has been found that it is preferable to utilize a pressure of about 750 W, an RF power of about 750 W and a time of about 25 to about 45 seconds.
[0025]
A method for forming a borderless via according to an embodiment of the present invention includes a step of forming a first insulating layer on a semiconductor substrate, and a metal separated by a wiring space by patterning the first metal layer on the first insulating layer. Forming a metal portion separated by a gap, such as a line. Next, the gap is filled by depositing HSQ, for example, at a suitable temperature of about 200 ° C., for example, by spinning using a conventional spin device utilized for SOG. HSQ can easily fill even gaps less than 0.15 microns completely without voids. Next, a second insulating layer is deposited on the first patterned metal layer and HSQ layer. Next, misaligned through holes are formed in the second insulating layer and partially penetrate the HSQ layer to form at least part of the side surface and part of the upper surface of the first metal layer and the HSQ layer. To expose a part of.
[0026]
Through-holes are formed by depositing a photoresist mask on the second insulating layer and etching through the photoresist mask and part of the HSQ layer. The photoresist mask is removed using O 2 containing plasma in a conventional manner, thereby degrading the HSQ layer. A degraded HSQ layer contains significantly fewer Si—H bonds and significantly more Si—OH bonds than an intact, freshly deposited HSQ layer. Further, when exposed to O 2 containing plasma, the degraded HSQ film shows an increase in moisture content, and the moisture content continues to increase by absorbing moisture from the surroundings.
[0027]
After removing the photoresist mask with O 2 containing plasma, the degraded HSQ layer is treated with H 2 / N 2 containing plasma, which significantly increases the number of Si—H bonds and significantly increases the number of Si—OH bonds. Decrease. Furthermore, during treatment with H 2 containing plasma, the moisture content of HSQ is reduced and the treated HSQ does not exhibit the critical property of absorbing moisture. By reversing the degradation caused by exposure to the O 2 containing plasma, the HSQ layer is substantially recovered and then the misaligned through holes are filled with a conductive material, such as a composite plug. Initially, a titanium, titanium nitride, titanium-tungsten or titanium-titanium nitride barrier is deposited, which serves as an adhesion promoter for subsequently deposited tungsten, which is a component of the main plug material. For example, a titanium-titanium nitride barrier material is sputter deposited using conventional sputtering equipment.
[0028]
In another embodiment of the invention, a CVD-TiN barrier layer is deposited according to the method disclosed in US Patent Application Serial No. 08 / 992,430, filed December 18, 1997. The advantage of this embodiment is that the H 2 / N 2 plasma treatment H 2 / N 2 plasma treatment and deposited CVD-TiN film of HSQ film may be made in the same chamber.
[0029]
A schematic diagram of an embodiment of the present invention is shown in FIG. The
[0030]
In this invention, the degraded HSQ layer is exposed to an H 2 containing plasma, thereby recovering the degraded HSQ layer by significantly increasing the number of Si—H bonds and significantly decreasing the number of Si—OH bonds. Let Furthermore, the recovered HSQ does not absorb much moisture from the surroundings. Next, the through
[0031]
After forming the conductive via 57, a second patterned metal layer is formed on the second insulating layer. The second metal layer includes a
[0032]
The metal layer utilized in this invention is consistent with the prior art and typically includes aluminum or an aluminum alloy. Embodiments of the present invention include a composite patterning that initially includes a refractory metal layer such as tungsten, titanium or titanium nitride, an intermediate aluminum or aluminum alloy layer, and a top antireflective coating such as titanium-titanium nitride. Forming a formed metal layer. In this invention, tungsten is deposited by conventional CVD techniques.
[0033]
The present invention can be applied to various types of semiconductor devices, especially fine portions, particularly high density multi-metal patterned layers with fine portions of 0.25 microns or less, exhibiting high speed features and improved reliability. The present invention allows for advantageous utilization of HSQ and can gap fill a patterned metal layer without the deleterious effects of process induced degradation, such as caused by exposure to an O 2 containing plasma. Thus, the present invention solves the problem of void formation in HSQ during borderless via formation. The invention is cost effective and can be easily integrated into conventional processes and equipment.
[0034]
In the embodiment of the present invention, the metal layer is made of a semiconductor such as aluminum, aluminum alloy, copper, copper alloy, gold, gold alloy, silver, silver alloy, refractory metal, refractory metal alloy and refractory metal compound. It can be formed from any metal typically utilized in device manufacture. The metal layer of the present invention can be formed by any technique conventionally used in the manufacture of semiconductor devices. For example, the metal layer can be formed by conventional metallization techniques such as conventional physical vapor deposition (PVD) or chemical vapor deposition (CVD) and electroplating of copper and copper alloys, for example.
[0035]
In the above description, numerous specific details are set forth such as specific materials, structures, chemical products, methods, etc., in order to provide a thorough understanding of the present invention. However, as will be appreciated by one skilled in the art, the invention may be practiced without resorting to the details specifically set forth. In other instances, well known processing features have not been described in order not to unnecessarily obscure the present invention.
[0036]
Only the preferred embodiment of the invention and an example of its versatility are shown and described in this disclosure. It should be understood that the invention can be used in a variety of other combinations and environments, and that changes and modifications can be made within the scope of the inventive concept as presented herein.
[Brief description of the drawings]
FIG. 1 is a schematic diagram illustrating gap filling of a conventional patterned metal layer.
FIG. 2 is a schematic diagram illustrating gap filling of a conventional patterned metal layer.
FIG. 3 is a schematic view illustrating a conventional metal plug via wiring.
FIG. 4 is a schematic diagram illustrating spikes in a borderless via.
FIG. 5 is a schematic diagram illustrating a borderless via formed according to the present invention.
Claims (18)
前記第1の絶縁層上に間隙を有する第1のパターニングされた金属層を形成するステップであって、前記第1のパターニングされた金属層は上部表面および側部表面を有する第1の金属部分を含むステップと、
Si−H結合を含有するハイドロゲンシラセスキオキサン(HSQ)層を堆積して前記間隙を充填するステップと、前記第1のパターニングされた層およびHSQ層上に第2の絶縁層を堆積するステップと、
スルーホールを前記第2の絶縁層中に形成して前記第1の金属部分の上部表面の一部と、前記第1の金属部分の側部表面の少なくとも一部と、を露出させ、前記HSQ層の一部を貫通し、露出させるステップと、
前記HSQ層をH2含有プラズマで処理しSi−H結合の数を増加させるステップと、
前記スルーホールを導電性材料で充填しボーダレスバイアを形成するステップとを含む、半導体装置の製造方法。Forming a first insulating layer on a semiconductor substrate;
Forming a first patterned metal layer with a gap on the first insulating layer, the first patterned metal layer having a top surface and a side surface; Including steps,
Depositing a hydrogen silsesquioxane (HSQ) layer containing Si-H bonds to fill the gap; and depositing a second insulating layer over the first patterned layer and the HSQ layer; ,
A through hole is formed in the second insulating layer to expose a portion of the upper surface of the first metal portion and at least a portion of the side surface of the first metal portion, and the HSQ Penetrating and exposing a portion of the layer;
Treating the HSQ layer with a H 2 containing plasma to increase the number of Si—H bonds;
Filling the through hole with a conductive material to form a borderless via.
エッチングしてスルーホールを形成するステップと、
フォトレジストマスクを除去するステップと、
フォトレジストマスク除去後に前記HSQ層をH2含有プラズマで処理するステップとを含む、請求項1に記載の方法。Forming a photoresist mask on the second insulating layer;
Etching to form a through hole; and
Removing the photoresist mask;
Treating the HSQ layer with an H 2 containing plasma after removing a photoresist mask.
上部の反射防止膜とを含む複合物である、請求項1に記載の方法。The first metal layer comprises a lower refractory metal layer, an intermediate layer of aluminum or aluminum alloy,
The method of claim 1, which is a composite comprising an upper antireflective coating.
前記第1の絶縁層上に形成される間隙を有する第1のパターニングされた金属層であって、上部表面および側部表面を有する第1の下部金属構造を含む金属層と、
前記間隙を充填するハイドロゲンシラセスキオキサン(HSQ)の層と、
前記第1のパターニングされた金属層上および前記HSQ層上に形成される第2の絶縁層と、
前記第2の絶縁層中に形成され、前記第1の下部金属構造の上部表面の一部と、前記第1の下部金属構造の側部表面の少なくとも一部と、を露出させ、前記HSQ層の一部を貫通し、露出させるスルーホールと、
前記スルーホールを充填することによりボーダレスバイアを形成し、前記第1の下部金属部分と第2の上部金属部分との間に電気的接続を形成する、導電性材料とを含み、
前記HSQ層は前記第1の金属部分および前記導電性材料に隣接し、
前記スルーホールは、
前記第2の絶縁層上にフォトレジストマスクを堆積し、
エッチングし、
前記HSQ層のSi−H結合の数の削減を引き起こすO2含有プラズマを用いて前記フォトレジストマスクを除去することによって形成され、
前記スルーホールを導電性材料で充填する前に、前記HSQ層をH 2 含有プラズマで処理してSi−H結合の数を増加させる、配線パターンを備える半導体装置。A first insulating layer on a semiconductor substrate;
A first patterned metal layer having a gap formed on the first insulating layer, the metal layer comprising a first lower metal structure having an upper surface and a side surface;
A layer of hydrogen silsesquioxane (HSQ) filling the gap;
A second insulating layer formed on the first patterned metal layer and on the HSQ layer;
An HSQ layer formed in the second insulating layer, exposing a portion of an upper surface of the first lower metal structure and at least a portion of a side surface of the first lower metal structure; A through hole that penetrates and exposes a portion of
A conductive material that forms a borderless via by filling the through-hole and forms an electrical connection between the first lower metal portion and the second upper metal portion;
The HSQ layer is adjacent to the first metal portion and the conductive material;
The through hole is
Depositing a photoresist mask on the second insulating layer;
Etched,
Formed by removing the photoresist mask using an O 2 containing plasma that causes a reduction in the number of Si—H bonds in the HSQ layer;
A semiconductor device comprising a wiring pattern in which the HSQ layer is treated with H 2 containing plasma to increase the number of Si—H bonds before filling the through holes with a conductive material .
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US08/951,592 US5866945A (en) | 1997-10-16 | 1997-10-16 | Borderless vias with HSQ gap filled patterned metal layers |
US08/951,592 | 1997-10-16 | ||
PCT/US1998/022040 WO1999019904A1 (en) | 1997-10-16 | 1998-10-16 | Borderless vias with hsq gap filled patterned metal layers |
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US6218078B1 (en) * | 1997-09-24 | 2001-04-17 | Advanced Micro Devices, Inc. | Creation of an etch hardmask by spin-on technique |
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WO1999019904A1 (en) | 1999-04-22 |
US6060384A (en) | 2000-05-09 |
DE69841696D1 (en) | 2010-07-15 |
EP1029344B1 (en) | 2010-06-02 |
EP1029344A1 (en) | 2000-08-23 |
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